FDA 510(k)

MODIFIED CORDIS PTCA GUIDING CATHETERS

K-Number: K854576 · 1986-02-26

Decision Date1986-02-26

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODIFIED CORDIS PTCA GUIDING CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K854576. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CORDIS PTCA GUIDING CATHETERS?

MODIFIED CORDIS PTCA GUIDING CATHETERS is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Cordis Corp.. The 510(k) number is K854576.

When did MODIFIED CORDIS PTCA GUIDING CATHETERS receive FDA 510(k) clearance?

MODIFIED CORDIS PTCA GUIDING CATHETERS received FDA 510(k) clearance on 1986-02-26, under 510(k) number K854576.

Who is the listed applicant for MODIFIED CORDIS PTCA GUIDING CATHETERS?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED CORDIS PTCA GUIDING CATHETERS?

The FDA product code for MODIFIED CORDIS PTCA GUIDING CATHETERS is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.